GTR Test Accession:
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GTR000561285.1
Registered in GTR:
2018-07-17
View version history
GTR000561285.1,
registered in GTR:
2018-07-17
Last annual review date for the lab: 2024-08-14
LinkOut
At a Glance
Test purpose:
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Diagnosis;
Screening
Conditions (2):
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Delta-0-thalassemia;
beta Thalassemia
Genes (4):
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HBB (11p15.4);
HBD (11p15.4);
HBG1 (11p15.4);
HBG2 (11p15.4)
Methods (1):
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Molecular Genetics - Deletion/duplication analysis: Multiplex Ligation-dependent Probe Amplification (MLPA)
Target population: Help
Multiplex Ligation-dependent Probe Amplification (MLPA) is an assay designed to …
Clinical validity:
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Not provided
Clinical utility:
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Not provided
Ordering Information
Offered by:
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Test short name:
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MLPA
Manufacturer's name:
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MRC-Holland
Specimen Source:
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- Buffy coat
- Dried blood spot (DBS) card
- Fetal blood
- Isolated DNA
- Peripheral (whole) blood
Who can order: Help
- Health Care Provider
Contact Policy:
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Laboratory can only accept contact from health care providers. Patients/families are encouraged to discuss genetic testing options with their health care provider.
How to Order:
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Test service:
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Clinical Testing/Confirmation of Mutations Identified Previously
Result interpretation
Result interpretation
Test development:
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Manufactured (research use only; not FDA-reviewed)
Informed consent required:
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Decline to answer
Pre-test genetic counseling required:
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Decline to answer
Post-test genetic counseling required:
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Decline to answer
Recommended fields not provided:
Test Order Code,
Lab contact for this test,
Test strategy
Conditions
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Total conditions: 2
Condition/Phenotype | Identifier |
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Test Targets
Genes
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Total genes: 4
Gene | Associated Condition | Germline or Somatic | Allele (Lab-provided) | Variant in NCBI |
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Methodology
Total methods: 1
Method Category
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Test method
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Instrument *
Deletion/duplication analysis
Multiplex Ligation-dependent Probe Amplification (MLPA)
* Instrument: Not provided
Clinical Information
Test purpose:
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Diagnosis;
Screening
Target population:
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Multiplex Ligation-dependent Probe Amplification (MLPA) is an assay designed to detect copy number changes (deletions and duplications) in β-globin gene cluster.
Recommended fields not provided:
Clinical validity,
Clinical utility,
What is the protocol for interpreting a variation as a VUS?,
Are family members with defined clinical status recruited to assess significance of VUS without charge?,
Will the lab re-contact the ordering physician if variant interpretation changes?,
Is research allowed on the sample after clinical testing is complete?,
Sample negative report,
Sample positive report
Technical Information
Availability:
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Tests performed
Entire test performed in-house
Entire test performed in-house
Analytical Validity:
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greater than 99%
Proficiency testing (PT):
Is proficiency testing performed for this test?
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No
No
Recommended fields not provided:
Test Confirmation,
Assay limitations,
Description of internal test validation method,
Citations for Analytical validity,
PT Provider,
Description of PT method,
Major CAP category, CAP category, CAP test list
Regulatory Approval
FDA Review:
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Category:
FDA exercises enforcement discretion
Additional Information
Reviews:
Clinical resources:
Consumer resources:
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Patients and consumers
with specific questions about a genetic test should contact a health care provider or a genetics professional.